Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1230950.RA9voWp9m1ikoS8jX_vcZA1DZkKBIJ3vugntf1cTogGxo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1230950.RA9voWp9m1ikoS8jX_vcZA1DZkKBIJ3vugntf1cTogGxo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1230950.RA9voWp9m1ikoS8jX_vcZA1DZkKBIJ3vugntf1cTogGxo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1230950.RA9voWp9m1ikoS8jX_vcZA1DZkKBIJ3vugntf1cTogGxo130_provenance.
- NP1230950.RA9voWp9m1ikoS8jX_vcZA1DZkKBIJ3vugntf1cTogGxo130_assertion description "[Recently, we identified a rare, nonsynonymous Slc6a3 variant that produces the DAT substitution Ala559Val in two male siblings who share a diagnosis of attention-deficit hyperactivity disorder (ADHD), with other studies identifying the variant in subjects with bipolar disorder (BPD) and autism spectrum disorder (ASD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1230950.RA9voWp9m1ikoS8jX_vcZA1DZkKBIJ3vugntf1cTogGxo130_provenance.
- NP1230950.RA9voWp9m1ikoS8jX_vcZA1DZkKBIJ3vugntf1cTogGxo130_assertion evidence source_evidence_literature NP1230950.RA9voWp9m1ikoS8jX_vcZA1DZkKBIJ3vugntf1cTogGxo130_provenance.
- NP1230950.RA9voWp9m1ikoS8jX_vcZA1DZkKBIJ3vugntf1cTogGxo130_assertion SIO_000772 25331903 NP1230950.RA9voWp9m1ikoS8jX_vcZA1DZkKBIJ3vugntf1cTogGxo130_provenance.
- NP1230950.RA9voWp9m1ikoS8jX_vcZA1DZkKBIJ3vugntf1cTogGxo130_assertion wasDerivedFrom befree-2016 NP1230950.RA9voWp9m1ikoS8jX_vcZA1DZkKBIJ3vugntf1cTogGxo130_provenance.
- NP1230950.RA9voWp9m1ikoS8jX_vcZA1DZkKBIJ3vugntf1cTogGxo130_assertion wasGeneratedBy ECO_0000203 NP1230950.RA9voWp9m1ikoS8jX_vcZA1DZkKBIJ3vugntf1cTogGxo130_provenance.
- befree-2016 importedOn "2016-02-19" NP1230950.RA9voWp9m1ikoS8jX_vcZA1DZkKBIJ3vugntf1cTogGxo130_provenance.